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Development of cell models for high-throughput screening system of Charcot-Marie-Tooth disease type 1

Choi YR, Jung SC, Shin J, Yoo SY, Lee JS, Joo J, Lee J, Hong YB, Choi BO

PURPOSE: Charcot-Marie-Tooth disease (CMT) is a peripheral neuropathy mainly divided into CMT type 1 (CMT1) and CMT2 according to the phenotype and genotype. Although molecular pathologies for each genetic causative...
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Myelin Protein Zero (MPZ) Gene Analysis in Korean Patients with Charcot-Marie-Tooth: Clinical and Electrophysiological Characteristics

Choi BO, Chung KW, Cho HJ, Park KD, Lee KS, Kim SM, Sunwoo IN

  • KMID: 2343145
  • J Korean Neurol Assoc.
  • 2005 Apr;23(2):227-231.
BACKGROUND: Mutations in the myelin protein zero (MPZ) gene, which is located on chromosome 1q21-q22, is present in Charcot-Marie-Tooth disease type 1B (CMT1B), CMT type 2, Dejerine-Sottas syndrome, and congenital...
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